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Tychele N Turner

Showing results (11-20 of 65) with videos related to

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Neurology. Genetics|July 12, 2023
Neurofibromatosis-1 Gene Mutational Profiles Differ Between Syndromic Disease and Sporadic CancersAlice F Bewley, Titilope M Akinwe, Tychele N Turner, et al.
Plant Communications|November 18, 2022
A gap-free genome assembly of Chlamydomonas reinhardtii and detection of translocations induced by CRISPR-mediated mutagenesisZachary L Payne, Gervette M Penny, Tychele N Turner, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Genome Medicine|November 29, 2017
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implicationsAmy B Wilfert, Arvis Sulovari, Tychele N Turner, et al.
Bioinformatics (Oxford, England)|October 3, 2021
ACES: Analysis of Conservation with an Extensive list of SpeciesEvin M Padhi, Jeffrey K Ng, Elvisa Mehinovic, et al.
Human Molecular Genetics|August 7, 2015
Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patternsTychele N Turner, Christopher Douville, Dewey Kim, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
High Coverage Highly Accurate Long-Read Sequencing of a Mouse Neuronal Cell Line Using the PacBio Revio SequencerJuana G Manuel, Hillary B Heins, Sandra Crocker, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 19, 2017
Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic riskAnne B Arnett, Brianna E Cairney, Arianne S Wallace, et al.
Molecular Autism|October 17, 2017
Clinical phenotype of ASD-associated <i>DYRK1A</i> haploinsufficiencyRachel K Earl, Tychele N Turner, Heather C Mefford, et al.
Cold Spring Harbor Molecular Case Studies|June 14, 2020
Precise breakpoint detection in a patient with 9p- syndromeJeffrey Ng, Eleanor Sams, Dustin Baldridge, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Neurology. Genetics|July 12, 2023
Neurofibromatosis-1 Gene Mutational Profiles Differ Between Syndromic Disease and Sporadic CancersAlice F Bewley, Titilope M Akinwe, Tychele N Turner, et al.
Plant Communications|November 18, 2022
A gap-free genome assembly of Chlamydomonas reinhardtii and detection of translocations induced by CRISPR-mediated mutagenesisZachary L Payne, Gervette M Penny, Tychele N Turner, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Genome Medicine|November 29, 2017
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implicationsAmy B Wilfert, Arvis Sulovari, Tychele N Turner, et al.
Bioinformatics (Oxford, England)|October 3, 2021
ACES: Analysis of Conservation with an Extensive list of SpeciesEvin M Padhi, Jeffrey K Ng, Elvisa Mehinovic, et al.
Human Molecular Genetics|August 7, 2015
Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patternsTychele N Turner, Christopher Douville, Dewey Kim, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
High Coverage Highly Accurate Long-Read Sequencing of a Mouse Neuronal Cell Line Using the PacBio Revio SequencerJuana G Manuel, Hillary B Heins, Sandra Crocker, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 19, 2017
Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic riskAnne B Arnett, Brianna E Cairney, Arianne S Wallace, et al.
Molecular Autism|October 17, 2017
Clinical phenotype of ASD-associated <i>DYRK1A</i> haploinsufficiencyRachel K Earl, Tychele N Turner, Heather C Mefford, et al.
Cold Spring Harbor Molecular Case Studies|June 14, 2020
Precise breakpoint detection in a patient with 9p- syndromeJeffrey Ng, Eleanor Sams, Dustin Baldridge, et al.
Pageof 7